HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Chlorothiophenol → HCID 58579932, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 58579849 | HCID 58579849 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58579932 | HCID 58579932 | 47% |
Reaction Steps
To a solution of tert-butyl 4-(hydroxymethyl)-6-oxopyridazine-1(6H)-carboxylate Part B (185 mg, 0.82 mmol) and Et3N (0.34 mL, 2.45 mmol) in CH2Cl2 (5 mL) under nitrogen at −10° C. was added a solution of methanesulfonyl chloride (0.076 mL, 0.98 mmol) in CH2Cl2 (2 mL). After stirring at RT for 15 min, 4-chlorobenzenethiol (355 mg, 2.45 mmol) was added to the reaction and the stirring at RT continued for 3 days. Following removal of the volatiles under vacuum, the crude product was purified by flash chromatography (silica gel/hexane-EtOAc 100:0 to 50:50 gradient, using LC-MS to identify fractions containing the desired product) to afford tert-butyl 4-((4-chlorophenylthio)methyl)-6-oxopyridazine-1(6H)-carboxylate 7C (137 mg, 47% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08278316B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-88765b7a26a249e780968736c6809564 |
| Source note | uspto-grants-2012_10 |